Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
4 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Publication Date timeline is not available.
Page 1
A recurrent de novo CUX2 missense variant associated with intellectual disability, seizures, and autism spectrum disorder.
Eur J Hum Genet. 2018 Sep;26(9):1388-1391. doi: 10.1038/s41431-018-0184-5. Epub 2018 May 24.
Eur J Hum Genet. 2018.
PMID: 29795476
Free PMC article.
Ghrelin-mediated inhibition of the TSH-stimulated function of differentiated human thyrocytes ex vivo.
Barington M, Brorson MM, Hofman-Bang J, Rasmussen ÅK, Holst B, Feldt-Rasmussen U.
Barington M, et al.
PLoS One. 2017 Sep 20;12(9):e0184992. doi: 10.1371/journal.pone.0184992. eCollection 2017.
PLoS One. 2017.
PMID: 28931076
Free PMC article.
Item in Clipboard
Novel Alu insertion in the ZEB2 gene causing Mowat-Wilson syndrome.
Barington M, Bak M, Kjartansdóttir KR, Hansen TVO, Birkedal U, Østergaard E, Hove HB.
Barington M, et al.
Am J Med Genet A. 2024 Aug;194(8):e63581. doi: 10.1002/ajmg.a.63581. Epub 2024 Apr 11.
Am J Med Genet A. 2024.
PMID: 38600862
Item in Clipboard
Homozygous splice variant (c.1741-6G>A) of the COL6A1 gene in three patients with Ullrich congenital muscular dystrophy.
Barington M, Dunø M, Birkedal U, Vissing J, Born AP, Krag T, Hansen TVO, Østergaard E.
Barington M, et al.
Neuromuscul Disord. 2023 Jul;33(7):539-545. doi: 10.1016/j.nmd.2023.05.007. Epub 2023 May 24.
Neuromuscul Disord. 2023.
PMID: 37315421
Free article.
Item in Clipboard
Cite
Cite
ARTICLE TYPE
ARTICLE LANGUAGE
AGE
Filters on the sidebar will be reset to the default list and any currently applied filters will be cleared.